Docking, synthesis and biological evaluation of pyridine ring containing Diaryl urea derivatives as anticancer agents

https://doi.org/10.53730/ijhs.v6nS3.6200

Authors

  • Vanita Marvaniya Research Scholar, Sankalchand Patel University, Visnagar, Gujarat, India
  • Hirak V. Joshi Faculty of Pharmacy, Sankalchand Patel University, Visnagar, Gujarat, India
  • Ujashkumar A. Shah Faculty of Pharmacy, Sankalchand Patel University, Visnagar, Gujarat, India
  • Jayvadan K. Patel Faculty of Pharmacy, Sankalchand Patel University, Visnagar, Gujarat, India
  • Jimish R. Patel Department of Pharmaceutical Chemistry, Shri B M Shah College of Pharmaceutical Education and Research, College Campus, Dhansura Road, Modasa-383315, Gujarat, India

Keywords:

pyridine, diaryl urea, molecular docking, anticancer, MTT assay

Abstract

A novel series of pyridine ring containing diaryl urea derivatives (R1-R9) were synthesized in four chemical steps using pyridine-2-carboxylic acid as starting material. The synthesized compounds were design by using Autodock vina in the crystal structure of the Kinase domain of Human B-raf (PDB ID: 4DBN) to get insights into structural requirements for anticancer activity. In vitro anticancer activity against cell line (MCF-7) showed that compounds R3, R6 and R9 were found to be the most potent (Docking score: > -12, IC50 = 17.39 µM) among the synthesized molecules.

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References

Anjaneyulu V, Krishnaiah V, RajeshKumar K and Leelavathi P, An Efficient One Pot Multicomponent Synthesis of Dihydro Pyrazolyl Bithiazole Derivatives as Potential Anticancer Agents and Their Molecular Docking Studies.” Research Square., 20, 2022.

Supaluk P, Ratchanok P , Apilak W, Nujarin S, Veda P , Somsak R and Virapong P ,Roles of Pyridine and Pyrimidine Derivatives as Privileged Scaffolds in Anticancer Agents. Mini Rev Med Chem,17, 2007, 869-901.

Sarah, P.; David, M., et al.“Mechanisms of anticancer drugs”,ScottBrown's Otorhinolaryngology: Head and Neck Surgery 7 Ed; CRC Press, 2008; Vol. pp. 34-46. DOI: https://doi.org/10.1201/b15118-6

Sinthupoom N, Prachayasittikul V, Prachayasittikul S, Ruchirawat, S, Prachayasittikul V,Nicotinic acid and derivatives as multifunctional pharmacophores for medical applications.Eur. Food Res. Technol., 240, 20015, 1-17. DOI: https://doi.org/10.1007/s00217-014-2354-1

Barot, K, Jain, S., Kremer, L., Singh, S., Ghate, M. , Recent advances and therapeutic journey of coumarins: current status and perspectives. Med. Chem. Res.,24, 2015, 2771-2798. DOI: https://doi.org/10.1007/s00044-015-1350-8

Meropi S., Nikolaos L., et al.Synthesis, Docking Study and Kinase Inhibitory Activity of a Number of New Substituted Pyrazolo[3,4-c]pyridines. Chem. Pharm. Bull., 65, 2017, 66–81. DOI: https://doi.org/10.1248/cpb.c16-00704

Espinosa, E., Zamora, P., Feliu, J., Gonzalez B., et al.Classification of anticancer drugs—a new system based on therapeutic targets. Cancer Treat. Rev.,29, 2013, 515-523. DOI: https://doi.org/10.1016/S0305-7372(03)00116-6

Rajeev S. Samant and Lalita A. Shevde, Recent Advances in Anti-Angiogenic Therapy of Cancer. Oncotarget, 2, 2011, 122-134. DOI: https://doi.org/10.18632/oncotarget.234

Dobbelstein, M., Moll, U. Targeting tumour-supportive cellular machineries in anticancer drug development. Nat. Rev. Drug Discov.,13, 2014, 179-196. DOI: https://doi.org/10.1038/nrd4201

Pommier, Y., Leo, E., Zhang, H., Marchand, C., Topoisomerases and their poisoning by anticancer and antibacterial drugs. Chem. Biol., 17, 2010, 421-433. DOI: https://doi.org/10.1016/j.chembiol.2010.04.012

Chiablaem, K., Lirdprapamongkol K., Keeratichamroen S., Surarit R.,Curcumin Suppresses Vasculogenic Mimicry Capacity of Hepatocellular Carcinoma Cells through STAT3 and PI3K/AKT Inhibition. J. Anticancer Res., 34, 2014, 1857-1864.

Mohamed N, Hadia A., Hany S., Ibrahim D., Wagdy M., and Hatem A. Pyridine-Ureas as Potential Anticancer Agents: Synthesis and In Vitro Biological Evaluation.Molecules,23,20087, 1459. doi:10.3390/molecules23061459. DOI: https://doi.org/10.3390/molecules23061459

Wilhelm S., Carter C., LynchM., LowingerT.,Dumas J., Smith, R., Schwartz, B., Simantov, R., Kelley, S., Hepatocellular Carcinoma: Basic and Transitional Research.Nat. Rev. Drug Discov., 5, 2006,835–844 . DOI: https://doi.org/10.1038/nrd2130

DiGiulio, S. FDA Approves Stivarga for Advanced GIST. Oncol. Times., 35, 2013,12. DOI: https://doi.org/10.1097/01.COT.0000428635.32713.a9

Cui J.J., Tran-Dube M., Shen H., Nambu M., Kung P.P., Pairish M., Jia L., Meng J., Funk L., Botrous I., Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK).J. Med. Chem. 54, 2011, 6342–6363. DOI: https://doi.org/10.1021/jm2007613

Patel, J. R., Shah, U. A., et al. Exploring novel endothelin receptor blocker as anti-hypertensive agents identified from a natural drugs library using induced fit docking and biological assay. Med. Plants - Int. J. Phytomed. Relat. Ind. (3), 2020, 405-413. DOI: https://doi.org/10.5958/0975-6892.2020.00051.9

Rina Herowati et al. Molecular Docking Studies of Chemical Constituents of Tinospora cordifolia on Glycogen Phosphorylase. Procedia Chem.13,2014, 63 – 68. DOI: https://doi.org/10.1016/j.proche.2014.12.007

Samar Salam Qawoogha et al, Identification of potential anticancer phytochemicals against colorectal cancer by structure-based docking studies.J. Recept. Signal Transduct. Res.2020 1-9. DOI: 10.1080/10799893.2020.1715431. DOI: https://doi.org/10.1080/10799893.2020.1715431

Joshi, H. V., Patel, J. K., et al, In silico screening of natural compounds to identify lead as interleukin 17A receptor blockers as antihypertensive agents. Thai J. Pharm. Sci.,44(3), 2020, 168-173.

Wei Li1., Xin Zhai1., Zheng Zhong.,et al. Design, Synthesis and Evaluation of Novel Rhodanine containing Sorafenib Analogs as Potential Antitumor Agents.Pharm. Chem. Life Sci. 11.2011, 349–357. DOI 10.1002/ardp.201000326. DOI: https://doi.org/10.1002/ardp.201000326

LU Chen S., Tang K., LI Yan., et al.Synthesis and in vitro antitumor activities of novel benzyl urea analogues of sorafenib.Acta Pharmaceutica Sinica. 48 (5), 20132, 709 −717. DOI 0513-4870 (2013) 05-0709-09.

Xiangkai Kong,Zeyu Yao, et al. Design, synthesis and biological evaluation of thiourea and nicotinamide-containing sorafenib analogs as antitumor agents.Med Che Comm. 2015; 1-5. DOI: 10.1039/C4MD00536H. DOI: https://doi.org/10.1039/C4MD00536H

Chunjiang Wu.; Shan Xu.;et al. Design, synthesis and biological evaluation of phenylpicolinamide sorafenib derivatives as antitumor agents.Med Chem Res. 2017; DOI 10.1007/s00044-017-2045-0.

Balakrishna M., Lekkala Ravinda., et al. The significance of N-methylpicolinamides in the development of anticancer therapeutics: Synthesis and structure-activity relationship (SAR) studies. Bioorganic Chemistry. 86, 2019, 513–537. DOI: https://doi.org/10.1016/j.bioorg.2019.02.030

Dimov S., Mavrova, A., et al. Anti- cancer in Medicinal Chemistry (Formerly current Medicinal Chemnisrt- Anti Cancer Agents).21(11), 2021.1441-1450. DOI: https://doi.org/10.2174/1871520620666200721131431

Sanjeev Kumar., Ekta Lathwal.,et al. Synthesis of pyrazole based novel aurone analogs and their cytotoxic activity against MCF-7 Cell line. Chemical Data Collection. 2020; doi: https://doi.org/10.1016/j.cdc.2020.100. DOI: https://doi.org/10.1016/j.cdc.2020.100559

Amani G. A., Kareem A. M., et al. Biosynthesis, Characterization, and Evaluation of the Cytotoxic Effects of Biologically Synthesized Silver Nanoparticles from Cyperus conglomeratus Root Extracts on Breast Cancer Cell Line MCF-7. Biological Trace Element Research. 2019; https://doi.org/10.1007/s12011-019-01791-7. DOI: https://doi.org/10.1007/s12011-019-01791-7

Wenbao W., Di W.,et al. Synthesis of new sarsasapogenin derivatives with cytotoxicity and apoptosis-inducing activities in human breast cancer MCF-7 cells. Eur. J. Med. Chem.127. 2017,62-71. DOI: https://doi.org/10.1016/j.ejmech.2016.12.011

Published

17-04-2022

How to Cite

Marvaniya, V., Joshi, H. V., Shah, U. A., Patel, J. K., & Patel, J. R. (2022). Docking, synthesis and biological evaluation of pyridine ring containing Diaryl urea derivatives as anticancer agents. International Journal of Health Sciences, 6(S3), 2851–2865. https://doi.org/10.53730/ijhs.v6nS3.6200

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Section

Peer Review Articles